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C/EBP beta mediates RNA polymerase III-driven transcription of oncomiR-138 in malignant gliomas

机译:C /EBPβ在恶性胶质瘤中介导RNA聚合酶III驱动的oncomir-138的转录

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摘要

MicroRNA-138 (miR-138) is a pro-survival oncomiR for glioma stem cells. In malignant gliomas, dysregulated expression of microRNAs, such as miR-138, promotes Tumour initiation and progression. Here, we identify the ancillary role of the CCAAT/enhancer binding protein beta (C/EBP beta) as a transcriptional activator of miR-138. We demonstrate that a short 158 bp DNA sequence encoding the precursor of miR-138-2 is essential and sufficient for transcription of miR-138. This short sequence includes the A-box and B-box elements characteristic of RNA Polymerase III (Pol III) promoters, and is also directly bound by C/EBP beta via an embedded 'C/EBP beta responsive element' (CRE). CRE and the Pol III B-box element overlap, suggesting that C/EBP beta and transcription factor 3C (TFIIIC) interact at the miR-138-2 locus. We propose that this interaction is essential for the recruitment of the RNA Pol III initiation complex and associated transcription of the oncomiR, miR-138 in malignant gliomas.
机译:MicroRNA-138(miR-138)是胶质瘤干细胞的胰蛋白酶胰蛋白酶。在恶性胶质瘤中,MIR-138等微小RORNA的失调表达促进了肿瘤引发和进展。在这里,我们将CCAAT / Enhancer结合蛋白β(C / EBPβ)作为MIR-138的转录活化剂识别CCAAT / Engancer结合蛋白β(C / EBP)的辅助作用。我们证明,编码MiR-138-2的前体的短158bp DNA序列是必不可少的并且足以用于转录miR-138。该短序列包括RNA聚合酶III(POL III)启动子的A盒和B盒元件,并且还通过嵌入的'C / EBPβ响应元素'(CRE)直接受C / EBPβ结合。 CRE和POL III B盒元件重叠,表明C / EBPβ和转录因子3C(TFIIIC)在miR-138-2基因座中相互作用。我们提出这种相互作用对于募集RNA POL III引发复合复合复合复合物和相关转录的oncomir,MIR-138在恶性胶质瘤中的互动至关重要。

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